510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K883847Substantially Equivalent

Derata Medi-Jector V

Derata Corp., Minneapolis MN / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K883847 is the FDA 510(k) clearance record for DERATA MEDI-JECTOR V, a class II device, cleared for Derata Corp. on under FDA product code KZE (Injector, Fluid, Non-Electrically Powered). FDA records list 6 510(k) clearances for Derata Corp., from to . As of , FDA records show no recalls naming K883847.

Clearance record

Decision date
Received
(49 days to decision)
Product code
KZE Injector, Fluid, Non-Electrically Powered
Regulation
21 CFR 880.5430
Device class
Class II
Review panel
General Hospital
Applicant
Derata Corp. 6701 Pkwy. Cir. Suite 100, Minneapolis MN
Third party review
No

Clearances, product code KZE

Trailing 12 months

FDA records hold no clearances under product code KZE in the trailing twelve months.

FDA records show no clearances under product code KZE in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code KZE, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260